Canonical Allele Identifier: CA575861929
Gene: ABCB1 HGNC NCBI

Linked Data

dbSNP Id: rs1157056617

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.87530822_87530841del , CM000669.2:g.87530822_87530841del GRCh38
NC_000007.13:g.87160138_87160157del , CM000669.1:g.87160138_87160157del GRCh37
NC_000007.12:g.86998074_86998093del NCBI36
NG_011513.1:g.187411_187430del

Transcript Alleles

HGVS Amino-acid Change
ENST00000265724.8:c.2685+456_2685+475del ENSP00000265724.3:n.2685+456_2685+475del
ENST00000622132.5:c.2685+456_2685+475del MANE Select ENSP00000478255.1:n.2685+456_2685+475del
ENST00000265724.7:c.2685+456_2685+475del ENSP00000265724.3:n.2685+456_2685+475del
ENST00000488737.6:n.327+456_327+475del
ENST00000496821.5:n.313+456_313+475del
ENST00000543898.5:c.2493+456_2493+475del ENSP00000444095.1:n.2493+456_2493+475del
ENST00000622132.4:c.2685+456_2685+475del ENSP00000478255.1:n.2685+456_2685+475del
NM_000927.4:c.2685+456_2685+475del NP_000918.2:n.2685+456_2685+475del
NM_001348944.1:c.2685+456_2685+475del NP_001335873.1:n.2685+456_2685+475del
NM_001348945.1:c.2895+456_2895+475del NP_001335874.1:n.2895+456_2895+475del
NM_001348946.1:c.2685+456_2685+475del NP_001335875.1:n.2685+456_2685+475del
NM_001348946.2:c.2685+456_2685+475del MANE Select NP_001335875.1:n.2685+456_2685+475del
NM_000927.5:c.2685+456_2685+475del NP_000918.2:n.2685+456_2685+475del
NM_001348944.2:c.2685+456_2685+475del NP_001335873.1:n.2685+456_2685+475del
NM_001348945.2:c.2895+456_2895+475del NP_001335874.1:n.2895+456_2895+475del